299926-07-1

Upstream product

• 30830-47-8 benzyl N-chlorocarbamate 
• 299926-03-7 (2S,3R)-tert-butyl 2-(tert-butyldimethylsilanyloxy)-3-(N-benzyloxycarbonyl)-aminobutanoate 
• 79218-15-8 tert-butyl (E)-crotonate 
• 299926-05-9 (2S,3R)-tert-Butyl 2-tert-butyldimethylsilyloxy-3-(N-benzyloxycarbonyl-N-methyl)aminobutanoate 

Downstream Products

• 299926-09-3 (1S,2R)-2-(N-Benzyloxycarbonyl-N-methyl)amino-1-(tert-butoxycarbonyl)propyl-1-methanesulfonate 
• 859235-76-0 (2S,3R)-3-(benzyloxycarbonyl-N-methylamino)-2-hydroxybutyric acid 
• 859235-83-9 methyl (2S,3R)-3-(benzyloxycarbonyl-N-methylamino)-2-hydroxybutyrate 
• 859235-79-3 methyl (2S,3R)-2-azido-3-(benzyloxycarbonyl-N-methylamino)butyrate 
• 859235-92-0 (2R,3R)-3-Methylamino-2-(4-methyl-benzyloxycarbonylamino)-butyric acid methyl ester 
• 859235-85-1 (2S,3R)-3-(Benzyloxycarbonyl-methyl-amino)-2-methanesulfonyloxy-butyric acid methyl ester 
• 859235-87-3 (2R,3R)-3-(Benzyloxycarbonyl-methyl-amino)-2-tert-butoxycarbonylamino-butyric acid methyl ester 
• 859235-80-6 (2R,3R)-3-[(9H-Fluoren-9-ylmethoxycarbonyl)-methyl-amino]-2-(4-methyl-benzyloxycarbonylamino)-butyric acid methyl ester 
• 859235-93-1 (2S,4R)-2-{[(1R,2R)-2-Methoxycarbonyl-1-methyl-2-(4-methyl-benzyloxycarbonylamino)-ethyl]-methyl-carbamoyl}-4-((Z)-propenyl)-pyrrolidine-1-carboxylic acid tert-butyl ester 
• 859235-94-2 (2S,4R)-2-{[(1R,2R)-2-Carboxy-1-methyl-2-(4-methyl-benzyloxycarbonylamino)-ethyl]-methyl-carbamoyl}-4-((Z)-propenyl)-pyrrolidine-1-carboxylic acid tert-butyl ester 
• 859236-04-7 [5-sec-butyl-18,19-dimethyl-11-(2-nitro-cyclopropylmethyl)-4,7,10,13,16,20-hexaoxo-8,14-bis-(1-phenyl-ethyl)-2-propenyl-eicosahydro-3a,6,9,12,15,19-hexaaza-cyclopentacyclononadecen-17-yl]-carbamic acid 4-methyl-benzyl ester 
• 859236-15-0 C₅₇H₈₂N₁₀O₁₃Si 
• 859236-16-1 C₅₈H₇₆ClN₁₁O₁₄ 
• 299926-11-7 (2R,3R)-tert-Butyl 2-azido-3-(N-benzyloxycarbonyl-N-methyl)aminobutanoate 

Relevant academic research and scientific papers

The structure of hormaomycin and one of its all-peptide aza- analogues in solution: Syntheses and biological activities of new hormaomycin analogues

Four new aza-analogues of hormaomycin 1, a secondary metabolite with interesting biological activities produced by Streptomyces griseoflavus, were synthesized and subjected to preliminary tests of their antibiotic activity to provide new insights into the

Synthesis of (S,S)- and (R,R)- 2-amino-3-methylaminobutanoic acid (AMBA)

The synthesis and characterization of (S, S)- and (R, R)-2-amino-3-methylaminobutanoic acid starting from tert-butyl crotonate is described.